Canonical Allele Identifier: CA779336977

Gene:

Linked Data

• dbSNP Id: rs1368463554
• MyVariant Identifiers: chr18:g.39057748_39057750del (hg19) ; chr18:g.41477784_41477786del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.41477792_41477794del , CM000680.2:g.41477792_41477794del	GRCh38
NC_000018.9:g.39057756_39057758del , CM000680.1:g.39057756_39057758del	GRCh37
NC_000018.8:g.37311754_37311756del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935409.1:n.86-26342_86-26340del